TY - JOUR
T1 - Affinity maturation of NZB and BALB/cV mice anti-fluorescyl response
AU - Jarvis, Michael R.
AU - Casperson, Gerald F.
AU - Kranz, David M.
AU - Voss, Edward W.
N1 - Funding Information:
* This work was supported in part by National Science Foundation Grant 76-16650. t To whom correspondence should be addressed. $ Abbreviations: Ka, average association constant; Kr, relative association constant determined by FQA; Cr, relative concentration of anti-fluorescein antibody; FU, fluorescence units; FF, fraction of fluorescence; F(I), protein-conjugated fluorescein, isomer I; KLH, keyhole limpet hemocyanin; FDS, fluorescein disodium salt; T,, T-suppressor; T,,, T-helper; PB, phosphate buffer; NTA, natural thymocytotoxic autoantibody.
PY - 1982/4
Y1 - 1982/4
N2 - Immunoglobulin affinity maturation of the anti-fluorescyl response was assessed with time and compared in groups (12 weeks old) of New Zealand Black (NZB) and BALB/cV mice, following intraperitoneal immunization with 100 μg of F(I)220 KLH per 15g of body weight. Affinity measurements were based on the quantitation of fluorescence quenching of fluorescein when specifically bound by immunoglobulin, and were expressed as relative association constants (Krs). Although Kr varied significantly within each group of mice, quantitative and qualitative differences in the pattern of affinity maturation between the two strains of mice were evident. NZB mice demonstrated a relatively more rapid increase in Kr and attained a higher average Kr for the primary response than BALB/cV mice. Thus, the NZB primary response resembled the BALB/cV secondary response kinetically and in the extent of affinity maturation. Secondary immunization of NZB mice did not result in an increase in affinity relative to the primary response. In contrast, reimmunization of BALB/cV mice produced a secondary anti-fluorescyl response of significantly higher affinity than the primary one. Comparison of affinity maturation patterns between the two mouse strains indicated a significant difference in responding lymphocyte populations. Since Ts activity in young NZB mice is known to be defective, a possible role for Ts function in the process of affinity maturation is discussed.
AB - Immunoglobulin affinity maturation of the anti-fluorescyl response was assessed with time and compared in groups (12 weeks old) of New Zealand Black (NZB) and BALB/cV mice, following intraperitoneal immunization with 100 μg of F(I)220 KLH per 15g of body weight. Affinity measurements were based on the quantitation of fluorescence quenching of fluorescein when specifically bound by immunoglobulin, and were expressed as relative association constants (Krs). Although Kr varied significantly within each group of mice, quantitative and qualitative differences in the pattern of affinity maturation between the two strains of mice were evident. NZB mice demonstrated a relatively more rapid increase in Kr and attained a higher average Kr for the primary response than BALB/cV mice. Thus, the NZB primary response resembled the BALB/cV secondary response kinetically and in the extent of affinity maturation. Secondary immunization of NZB mice did not result in an increase in affinity relative to the primary response. In contrast, reimmunization of BALB/cV mice produced a secondary anti-fluorescyl response of significantly higher affinity than the primary one. Comparison of affinity maturation patterns between the two mouse strains indicated a significant difference in responding lymphocyte populations. Since Ts activity in young NZB mice is known to be defective, a possible role for Ts function in the process of affinity maturation is discussed.
UR - http://www.scopus.com/inward/record.url?scp=0020054757&partnerID=8YFLogxK
U2 - 10.1016/0161-5890(82)90220-6
DO - 10.1016/0161-5890(82)90220-6
M3 - Article
C2 - 6211610
AN - SCOPUS:0020054757
SN - 0161-5890
VL - 19
SP - 525
EP - 533
JO - Molecular Immunology
JF - Molecular Immunology
IS - 4
ER -